Canonical Allele Identifier: CA2175529437
Gene: FBN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48509055G= , CM000677.2:g.48509055G= GRCh38
NC_000015.9:g.48801252G= , CM000677.1:g.48801252G= GRCh37
NC_000015.8:g.46588544G= NCBI36
NG_008805.2:g.141734C= , LRG_778:g.141734C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559133.6:c.1715-351C= ENSP00000453958.2:n.1715-351C=
ENST00000674301.2:c.1715-351C= ENSP00000501333.2:n.1715-351C=
ENST00000684448.1:n.389-351C=
ENST00000316623.10:c.1715-351C= MANE Select ENSP00000325527.5:n.1715-351C=
ENST00000316623.9:c.1715-351C= ENSP00000325527.5:n.1715-351C=
ENST00000537463.6:c.636+28656C= ENSP00000440294.2:n.636+28656C=
NM_000138.4:c.1715-351C= , LRG_778t1:c.1715-351C= NP_000129.3:n.1715-351C=
NM_000138.5:c.1715-351C= MANE Select NP_000129.3:n.1715-351C=
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